A method of making a medical guidewire including providing a wire having a length that includes a proximal length and a distal length. The method further includes applying cold work to the distal length and not applying cold work to the proximal length, thereby imparting to the distal length a diameter that is smaller than the proximal length diameter; and applying a reducing process to the wire whereby the proximal length is reduced to have an outer diameter that is the same as the outer diameter of the distal length. The proximal length has an inner diameter and the distal length has an inner diameter that is less than the inner diameter of the proximal length.

One aspect relates to a guidewire system, a measuring system, and a method for manufacturing such guidewire system. The guidewire system includes a guidewire and a surface acoustic wave sensor device. A portion of a surface of the guidewire is coated by the surface acoustic wave sensor device. The surface acoustic wave sensor device may be configured for measuring a pressure change. The surface acoustic wave sensor device includes a piezoelectric substrate and a transducer. A thickness of the surface acoustic wave sensor device perpendicular to a longitudinal direction of the guidewire is smaller than 100 μm.

An apparatus and method of manufacture includes a helical wire coil and a core wire. The core wire has a first wire portion and a second wire portion. The first wire portion of the core wire extends through the helical wire coil. The second wire portion of the core wire is intertwined with the first helical wire coil to fixedly secure the core wire relative to the first helical wire coil. The core wire is formed from a first material that is non-extensible. The core wire is fixedly secured relative to a distal portion of the helical wire coil such that the core wire inhibits longitudinal elongation of the helical wire coil along a longitudinal coil axis.

One aspect is a medical guidewire including a core wire with a proximal end extending out to a distal end and a resilient portion coupled to the distal end of the core wire at a distal tip section of the guidewire. The resilient portion includes a superelastic material.

A guidewire includes an elongate core member having an intermediate segment, a distal segment and a proximal segment, a distal shoulder between the intermediate segment and the distal segment and a proximal shoulder between the intermediate segment and the proximal segment. A coil having a proximal end and a distal end is disposed about at least a portion of the distal segment of the elongate core member and disposed adjacent to the distal shoulder. A distal tip comprising a polymer material is disposed adjacent to the distal end of the coil and a proximal polymer member, the proximal polymer member disposed adjacent to the proximal shoulder. At least the intermediate segment and the coil have a diameter that is substantially the same.

A medical device, such as a medical wire, which includes a coating applied to the surface of the medical wire. The coating includes a base layer bonded to the surface of the medical wire and an at least partially transparent low-friction top coat applied to the base layer. The base layer includes heat activated pigments that change color when heated above a color shifting temperature. In one embodiment, the color of the pigment in one area contrasts with the color of the pigment in an adjacent area without otherwise affecting the low-friction surface of the coating. The areas of different color created in locations along the length of the low-friction coated medical wire form markings which, as an example, enable a surgeon to determine the length of the medical wire inserted into a body by observing the markings on the portion of the marked medical wire located exterior to the body.

A method of forming a fenestrated tubular support member includes determining a first iso-stiffness curve corresponding to a first function of beam length versus ring width for the first stiffness; determining a second iso-stiffness curve corresponding to a second function of beam length versus ring width for the second stiffness; determining an iso-volume curve corresponding to a third function of beam length versus ring width for a given fenestration volume; identifying a first intersection point where the iso-volume curve intersects the first iso-stiffness curve; and identifying a second intersection point where the iso-volume curve intersects the second iso-stiffness curve. The first section ring width and first section beam length are determined from the first intersection point, and the second section ring width and second section beam length are determined from the second intersection point.

A guidewire with a cross section of at least a part of its length, comprising a filling material (PLM), a lumen (LM) arranged inside the filling material (PLM) for accommodating an optical fiber (OF) with optical shape sensing properties. One or more stiffening elements (RD) are arranged inside the first material (PLM), wherein the stiffening element(s) (RD) is formed by a material having a higher axial stiffness than the filling material. A braiding structure (BR) encircles all of: the filling material (PLM), the lumen (LM), and the stiffening element(s) (RD). Such guidewire can be designed with a circular symmetric bending behavior, and is thus suitable as an interventional medical device, e.g. for endovascular procedures, and still it can provide optical shape sensing properties.

Disclosed herein are embodiments of segmented metallic guidewires that are suitable for MRI catheterization. Disclosed guidewires comprise a plurality of short conductive metallic segments that individually are short enough such that they do not resonate during MRI. The conductive segments are electrically insulated from each other and mechanically coupled together end-to-end via connectors, such as stiffness matched connectors, to provide a sufficiently long, strong, and flexible guidewire for catheterization that is non-resonant during MRI.

A guidewire made from a drawn filled tube composite wire is described. The composite wire has a stainless steel outer sheath jacketing a nitinol core wire. The drawn filled tube composite wire is ground at its distal end to expose the nitinol core, which has superelastic and kink resistant properties that are desirable for the distal end of a guidewire. The proximal end of the drawn filled tube is not ground or if ground, the outer sheath of stainless steel is not removed to an extent sufficient to expose the nitinol core.